Literature DB >> 13469165

Different types of hereditary optic atrophy.

P J WAARDENBURG.   

Abstract

Entities:  

Keywords:  EYE DISEASES/heredity; NERVES, OPTIC/diseases

Mesh:

Year:  1957        PMID: 13469165     DOI: 10.1159/000150987

Source DB:  PubMed          Journal:  Acta Genet Stat Med        ISSN: 0567-7440


× No keyword cloud information.
  7 in total

Review 1.  LEBER'S DISEASE IN THE NETHERLANDS.

Authors:  A H VANSENUS
Journal:  Doc Ophthalmol       Date:  1963       Impact factor: 2.379

2.  Bibliography of human genetics.

Authors:  R H POST
Journal:  Am J Hum Genet       Date:  1958-12       Impact factor: 11.025

Review 3.  Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.

Authors:  M Votruba; A T Moore; S S Bhattacharya
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

4.  Diagnostic and therapeutic problems in nystagmus.

Authors:  K Wybar
Journal:  Br J Ophthalmol       Date:  1969-04       Impact factor: 4.638

5.  Severe visual impairment in Swedish children.

Authors:  E Lindstedt
Journal:  Doc Ophthalmol       Date:  1972-04-15       Impact factor: 2.379

6.  Optic atrophy in childhood.

Authors:  J Wilson
Journal:  Proc R Soc Med       Date:  1967-02

Review 7.  A review of primary hereditary optic neuropathies.

Authors:  M Votruba; S Aijaz; A T Moore
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.